Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs1800775
CETP
0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 7
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 7
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 7
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 6
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 6
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 6
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs10830962 0.851 0.160 11 92965261 upstream gene variant C/A;G;T snv 4
rs11986942 1.000 0.040 8 20009934 intergenic variant C/G;T snv 4
rs1387153 0.807 0.200 11 92940662 downstream gene variant C/G;T snv 4
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 4
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs16940212
ALDH1A2
1.000 0.040 15 58401821 intron variant G/A;T snv 3
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 3
rs271
LPL
1.000 0.040 8 19956191 intron variant G/A;T snv 3
rs486394
LINC02702
1.000 0.040 11 116655605 intron variant A/C;T snv 3
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs7013777 1.000 0.040 8 20020845 intergenic variant T/C;G snv 3
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 3
rs11887534
ABCG5 ; ABCG8
0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 2
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 2